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NCT00203957 · ClinicalTrials.gov registry record · Phase 3

Study of KW-6002 (Istradefylline) in Parkinson's Disease in Patients With Motor Response Complications on Levodopa

A Phase 3 study of Parkinson's Disease, sponsored by University of Chicago.

Completed
Registry status
Phase 3
Development phase
10
Enrollment target
1
Study location

NCT00203957: Completed Phase 3 study of Parkinson's Disease, sponsored by University of Chicago.

NCT00203957 is a Phase 3 study of Parkinson's Disease that has completed, run by University of Chicago. The registered enrollment target is 10 participants, below the 635-participant average among 158 other Parkinson's Disease trials with a reported enrollment target (98% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00203957, a Phase 3 study of Parkinson's Disease, has completed, sponsored by University of Chicago.

COMPLETED
Registry status
Phase 3
Development phase
10 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to confirm the long term tolerability and safety of oral 20 or 40 mg/d doses of Istradefylline.

Conditions Studied

Interventions

  • DRUG Istradefylline

Study Locations (1)

Illinois

  • The University of Chicago - Chicago

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2005-03
Est. Completion 2007-02
Phase Phase 3
University of Chicago

796 total trials

What the finished NCT00203957 record still lists

NCT00203957 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 10 participants, a relatively small participant target, below the 635-participant average among 158 other Parkinson's Disease trials with a reported enrollment target (98% lower).

The record links to 1 condition, with Parkinson's Disease appearing as the primary indexed condition, and to 1 intervention - of which Istradefylline is the first listed.

NCT00203957 reports a single indexed study location in Illinois.

Frequently Asked Questions

What is clinical trial NCT00203957 about?

NCT00203957 is a clinical study titled "Study of KW-6002 (Istradefylline) in Parkinson's Disease in Patients With Motor Response Complications on Levodopa". The purpose of this study is to confirm the long term tolerability and safety of oral 20 or 40 mg/d doses of Istradefylline.

What is the current status of trial NCT00203957?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 10 participants. The study started on 2005-03. Estimated completion is 2007-02.

What conditions does trial NCT00203957 study?

This clinical trial studies the following conditions: Parkinson's Disease.

What interventions are being tested in trial NCT00203957?

The interventions under investigation include: Istradefylline (DRUG).

Who is sponsoring clinical trial NCT00203957?

This trial is sponsored by University of Chicago, which has 796 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00203957 being conducted?

This trial has 1 study location across Illinois. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Parkinson's Disease

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00203957's enrollment target sits among peer trials

10 146th of 158 higher than 8 of 158 other Parkinson's Disease trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Parkinson's Disease trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00203957, the US trial registry maintained by the National Library of Medicine. NCT00203957 (small enrollment · single site footprint · completed) retrieved and formatted by PlainTrial, see methodology.